WO2016173927A1 - Topical sunscreen emulsions - Google Patents

Topical sunscreen emulsions Download PDF

Info

Publication number
WO2016173927A1
WO2016173927A1 PCT/EP2016/058931 EP2016058931W WO2016173927A1 WO 2016173927 A1 WO2016173927 A1 WO 2016173927A1 EP 2016058931 W EP2016058931 W EP 2016058931W WO 2016173927 A1 WO2016173927 A1 WO 2016173927A1
Authority
WO
WIPO (PCT)
Prior art keywords
topical sunscreen
sunscreen emulsion
topical
emulsion
phytantriol
Prior art date
Application number
PCT/EP2016/058931
Other languages
English (en)
French (fr)
Inventor
Cyrille Deshayes
Christine Mendrok-Edinger
Original Assignee
Dsm Ip Assets B.V.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Dsm Ip Assets B.V. filed Critical Dsm Ip Assets B.V.
Priority to JP2017555390A priority Critical patent/JP6798664B2/ja
Priority to US15/568,557 priority patent/US10709649B2/en
Priority to ES16720758T priority patent/ES2746287T3/es
Priority to EP16720758.8A priority patent/EP3288525B1/en
Priority to BR112017023041-0A priority patent/BR112017023041B1/pt
Priority to KR1020177032576A priority patent/KR20170141709A/ko
Priority to CN201680024320.8A priority patent/CN107530256B/zh
Publication of WO2016173927A1 publication Critical patent/WO2016173927A1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34Alcohols
    • A61K8/345Alcohols containing more than one hydroxy group
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/06Emulsions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/06Emulsions
    • A61K8/062Oil-in-water emulsions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/55Phosphorus compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q17/00Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
    • A61Q17/04Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations

Definitions

  • the invention relates to topical sunscreen emulsion comprising an oil phase and a water phase, wherein said emulsion comprises a cetyl phosphate emulsifier, phytantriol and an amount of at least 1 wt.-% based on the total weight of the topical sunscreen emulsion of at least one UV-filter substance. Furthermore, the invention relates to the use of phytantriol for improving the water resistance of such topical sunscreen emulsions.
  • UV-A radiation is equally or even more important in the development of solar damage and skin diseases, such as lupus erythematosus and melanoma and non-melanoma skin cancer.
  • SPF's Sun Protection Factor
  • Water resistance of sun care products is a key parameter for today's sunscreens and can for example be achieved by the addition of film forming polymers.
  • These film forming polymers are either not sufficiently effective and/ or render the product unattractive for the end consumer due to the resulting sensory properties as such products often exhibit an oily, dull, and sticky feeling on the skin as e.g. outlined in DE 102010063825.
  • the invention relates to topical sunscreen emulsions comprising an oil phase and a water phase, wherein said emulsion comprises a cetyl phosphate emulsifier, phytantriol and an amount of at least 1 wt.-% based on the total weight of the topical sunscreen emulsion of at least one UV-filter substance.
  • the invention relates to the use of phytantriol for increasing the water resistance of a topical sunscreen emulsion comprising at least one UV-filter substance.
  • the invention relates to a method for increasing the water resistance of at least one UV-filter substance in a topical sunscreen emulsion, said method comprising the addition of phytantriol into said topical sunscreen emulsion and, preferably, observing or appreciating the result.
  • the amount of phytantriol to be used in the topical sunscreen emulsions according to the invention should be selected such in order to achieve the stated results. Particular advantageous is a concentration of at least 0.05 wt.-% of phytantriol based on the total weight of the topical sunscreen emulsion.
  • the amount of phytantriol is, however, selected in the range of 0.1 to 3 wt.-%, more preferably in the range of 0.2 to 2 wt.-% and most preferably in the range of 0.3 to 1 .5 wt.-% based on the total weight of the topical sunscreen emulsion.
  • the amount of the UV-filter substances is preferably selected in the range of 1 to 40 wt.-%, more preferably in the range of 5 to 35 wt.-% and most preferably in the range of 10 to 30 wt.-% based on the total weight of the topical sunscreen emulsion.
  • the amount of the cetyl phosphate emulsifier is preferably selected in the range of 0.1 to 5 wt.-%, more preferably in the range of 0.25 to 2 wt.-% and most preferably in the range of 0.3 to 1 wt.-% based on the total weight of the topical sunscreen emulsion.
  • Suitable UV-filter substances according to the invention are UVA, UVB and/ or broadspectrum UV-filter substances which are or can be used as cosmetically acceptable UVA, UVB or broadspectrum UV-filter substances.
  • Such UV-filter substances are e.g. listed in the CTFA Cosmetic ingredient Handbook or "The Encyclopedia of Ultraviolet Filters” (ISBN: 978-1 -932633-25-2) by Nadim A. Shaath.
  • the UV-filter substances may be organic or inorganic compounds.
  • Exemplary UVA, UVB and/ or broadspectrum UV-filter substances encompass dibenzoylmethane derivatives such as e.g. butyl methoxydibenzoylmethane (PARSOL ® 1789); acrylates such as e.g. octocrylene (PARSOL ® 340); camphor derivatives such as e.g. 4-methyl benzylidene camphor (PARSOL ® 5000) or terephthalylidene dicamphor sulfonic acid (Mexoryl ® SX); cinnamate derivatives such as e.g.
  • ethylhexyl methoxycinnamate PARSOL ® MCX or isoamyl methoxycinnamate
  • p-aminobenzoic acid derivatives such as e.g. p-aminobenzoic acid or 2-ethylhexyl p-dimethylaminobenzoate
  • benzophenones such as e.g. benzophenone-3, benzophenone-4, 2,2',4,4'-tetrahydroxy-benzophenone or 2,2'- dihydroxy-4,4'-dimethoxybenzophenone
  • esters of benzalmalonic acid such as e.g.
  • organosiloxane compounds carrying chromophore groups such as e.g. polysilicone-15 (PARSOL ® SLX) or drometrizole trisiloxane (Mexoryl ® XL); imidazole derivatives such as e.g. 2-phenyl benzimidazole sulfonic acid and salts thereof such as e.g. its sodium- or potassium salts (PARSOL ® HS); salicylate derivatives such as e.g.
  • ethylhexyl salicylate PARSOL ® EHS, Neo Heliopan ® OS
  • isooctyl salicylate or homosalate PARSOL ® HMS, Neo Heliopan ® HMS
  • triazine derivatives such as e.g. ethylhexyl triazone (Uvinul ® T-150), diethylhexyl butamido triazone (Uvasorb ® HEB), bis-ethylhexyloxyphenol methoxyphenyl triazine (Tinosorb ® S) or 2,4,6-tris[1 ,1 '-biphenyl]-4-yl-1 ,3,5-triazine [CAS No.
  • Benzotriazole derivatives such as e.g. methylene bis-benzotriazolyl tetramethylbutylphenol (Tinosorb ® M); encapsulated UV-filters such as e.g. encapsulated ethylhexyl methoxycinnamate (Eusolex ® UV-pearls); amino substituted hydroxybenzophenones such as e.g. diethylamino hydroxybenzoyi hexyl benzoate (Aminobenzophenon, Uvinul ® A Plus); benzoxazol-derivatives such as e.g.
  • disodium phenyl dibenzimidazole tetrasulfonate (2,2- (1 ,4-phenylene)bis-(1 H-benzimidazol-4,6-disulfonic acid, Neoheliopan ® AP); 1 ,1 '-(1 ,4-piperazinediyl)bis[1 -[4-(diethylamino)-2-hydroxybenzoyl]phenyl]- methanone (CAS No. 919803-06-6); as well as Bis(butylbenzoate) diaminotriazine aminopropyltrisiloxane (CAS No. 207562-42-3).
  • Inorganic UV-filter substances encompass pigments such as e.g. microparticulated zinc oxide or titanium dioxide (e.g. commercially available as PARSOL ® TX)
  • microparticulated refers to a particle size from about 5 nm to about 200 nm, particularly from about 15 nm to about 100 nm.
  • the particles may also be coated by other metal oxides such as e.g. aluminum or zirconium oxides or by organic coatings such as e.g. polyols, methicone, aluminum stearate, alkyl silane. Such coatings are well known in the art.
  • Preferred UVB-filter substances to be incorporated into the topical sunscreen emulsions according to the invention encompass polysilicone-15, phenylbenzimidazol sulfonic acid, octocrylene, ethylhexyl methoxycinnamate, ethyl hexylsalicylate and/ or homosalate, most preferably phenyl benzimidazole sulfonic acid.
  • Preferred broadband UV-filter substances to be incorporated into the topical sunscreen emulsions according to the invention encompass unsymmetrical s-triazine derivatives such as in particular bis-ethylhexyloxyphenol methoxyphenyl triazine, certain benzophenones such as e.g. 2-hydroxy-4-methoxy-benzophenon, methylene bis-benzotriazolyl tetramethylbutylphenol and/ or titanium dioxide.
  • Preferred UVA-filter substances to be incorporated into the topical sunscreen emulsions according to the invention encompass butyl methoxydibenzoylmethane, diethylamino hydroxybenzoyi hexyl benzoate, 2,4-bis-[5- 1 (dimethylpropyl)benzoxazol-2-yl-(4-phenyl)-imino]-6-(2-ethylhexyl)-imino-1 ,3,5- triazine and/ or disodium phenyl dibenzimidazole tetrasulfonate, in particular butyl methoxydibenzoylmethane and/ or diethylamino hydroxybenzoyi hexyl benzoate.
  • topical sunscreen emulsions comprise butyl methoxydibenzoylmethane, then they advantageously contain in addition at least one suitable photostabilizer for butyl methoxydibenzoylmethane.
  • suitable photostabilizers encompass Polyester 8 (Polycrylene ® ); Methoxycrylene (Solastay); diethylhexyl syringylidene malonate (Oxynex ST liquid); diethylhexyl naphthalate (Corapan TQ) as well as Benzotriazolyl Dodecyl p-Cresol (Tinogard ® TL) without being limited thereto.
  • the topical sunscreen emulsions according to the invention comprise at least 2, more preferably at least 3, most preferably at least 4 different UV-filter substances.
  • the topical sunscreen emulsions according to the invention in addition, comprise at least one UV-B filter substance and at least one UVA-filter substance.
  • the at least one UV-filter substance present in the topical sunscreen emulsions according to the invention is selected from the group consisting of polysilicone-15, phenylbenzimidazol sulfonic acid, octocrylene, ethylhexyl methoxycinnamate, ethyl hexylsalicylate, homosalate, bis- ethylhexyloxyphenol methoxyphenyl triazine, methylene bis-benzotriazolyl tetramethylbutylphenol, titanium dioxide, butyl methoxydibenzoylmethane, diethylamino hydroxybenzoyl hexyl benzoate, disodium phenyl dibenzimidazole tetrasulfonate as well as mixtures thereof.
  • the at least one UV-filter substances is selected from the group consisting of butyl methoxydibenzoylmethane, phenyl benzimidazol sulfonic acid, polysilicone-15, octocrylene, homosalate, ethylhexyl salicylate, methylene bis-benzotriazolyl tetramethylbutylphenol as well as mixtures thereof.
  • the compositions comprises always phenyl benzimidazole sulfonic acid, optionally in combination with at least one further UV-filter substance with the preferences as outlined herein.
  • the topical sunscreen emulsions according to the invention comprise either a mixture of butyl methoxydibenzoylmethane, phenylbenzimidazol sulfonic acid, octocrylene, homosalate, and ethylhexyl salicylate or a mixture of butyl methoxydibenzoylmethane, phenylbenzimidazol sulfonic acid, octocrylene, and methylene bis-benzotriazolyl tetramethylbutylphenol as sole UV-filter substances.
  • the total amount of butyl methoxydibenzoylmethane, octocrylene, homosalate, methylene bis-benzotriazolyl tetramethylbutylphenol and ethylhexyl salicylate preferably sums up to 20 to 30 wt.-%, whereas the total amount of phenylbenzimidazol sulfonic acid is selected in the range of 1 to 3 wt.-%.
  • the UV-filter substances are incorporated either in the water or in oil phase of the topical sunscreen emulsion, depending if they are water or oil (fat) soluble/ miscible UV filter substances. They may even be added to the final emulsion by standard methods known to a person skilled in the art.
  • cetyl phosphate emulsifiers encompass Cetyl Phosphate, DEA-Cetyl Phosphate, Potassium cetyl phosphate, and mixtures thereof.
  • a particular preferred phosphate ester emulsifiers to be used in the topical sunscreen emulsions according to the invention is preferably potassium cetyl phosphate is e.g. commercially available as Amphisol ® K at DSM Nutritional Products Ltd Kaiseraugst.
  • topical sunscreen emulsions As the topical sunscreen emulsions according to the invention are intended for topical application, they comprise a cosmetically acceptable carrier i.e. a physiologically acceptable medium which is compatible with keratinous substances, such as in particular the skin.
  • a cosmetically acceptable carrier refers to all cosmetic carriers and/or excipients and/or diluents conventionally used in topical sunscreen emulsions.
  • the topical sunscreen emulsions of the invention can also contain further conventional cosmetic adjuvants and additives, such as preservatives/antioxidants, fatty substances/oils, water, organic solvents, silicones, thickeners, softeners, emulsifiers, antifoaming agents, aesthetic components such as fragrances, emulsifiers, fillers, sequestering agents, anionic, cationic, nonionic or amphoteric polymers or mixtures thereof, propellants, acidifying or basifying agents, dyes, colorings/colorants, abrasives, absorbents, chelating agents and/ or sequestering agents, essential oils, skin sensates, astringents, pigments or any other ingredients usually formulated into such compositions.
  • cosmetic adjuvants and additives such as preservatives/antioxidants, fatty substances/oils, water, organic solvents, silicones, thickeners, softeners, emulsifiers, antifoaming agents, aesthetic components such as fragrance
  • the topical sunscreen emulsions according to the invention may comprise further cosmetically active ingredients conventionally used in topical sunscreen emulsions.
  • active ingredients encompass skin lightening agents; agents for the treatment of hyperpigmentation; agents for the prevention or reduction of inflammation; firming, moisturizing, soothing, and/ or energizing agents as well as agents to improve elasticity and skin barrier.
  • cosmetic carriers, excipients, ingredients, adjuvants, diluents and additives commonly used in the skin care industry which are suitable for use in the compositions of the invention, are for example described in the International Cosmetic Ingredient Dictionary & Handbook by Personal Care Product Council (http://www.personalcarecouncil.org/), accessible by the online INFO BASE (http://online.personalcarecouncil.org/jsp/Home.jsp), without being limited thereto.
  • the necessary amounts of the active ingredients as well as the cosmetic adjuvants, diluents and additives can, based on the desired product form and application, easily be determined by the skilled person.
  • the additional ingredients can either be added to the oily phase, the aqueous phase or separately as deemed appropriate.
  • the cosmetically active ingredients useful herein can in some instances provide more than one benefit or operate via more than one mode of action.
  • the topical sunscreen emulsions according to the invention may be in the form of an oil-in-water (O/W), a water-in-oil (W/O) type, a silicone-in-water (Si/W), or a water-in-silicone (W/Si) emulsion. It can also be in the form of a PIT-emulsion, a multiple emulsion (e.g. oil-in-water-in oil (0/W/O) or water-in-oil-in-water (W/O/W)) or a pickering emulsion, which can of course also be in the form of a micro- emulsion.
  • O/W oil-in-water
  • W/O water-in-oil
  • W/Si water-in-silicone
  • the amount of the oil phase present in the topical sunscreen emulsions according to the invention is advantageously at least 10 wt.-%.
  • the amount of the oil phase in all embodiments of the present invention is selected in the range of 10 to 60 wt.-%, more preferably in the range of 20 to 50 wt.-% and most preferably in the range of 25 to 40 wt.-% based on the total weight of the topical sunscreen emulsion.
  • the oil phase encompasses the therein contained cosmetic oils as well as any oil (fat) soluble or miscible UV-filter substances.
  • the oil phase encompasses at least 12 wt.-%, more preferably at least 20 wt.-% such as most preferably about 25 wt.-% based on the total weight of the topical sunscreen emulsion of oil soluble or miscible UV-filter substances.
  • UV-filter substances are selected from the group consisting of polysilicone-15, octocrylene, ethylhexyl methoxycinnamate, ethyl hexylsalicylate, homosalate, bis-ethylhexyloxyphenol methoxyphenyl triazine, butyl methoxydibenzoylmethane, diethylamino hydroxybenzoyi hexyl benzoate as well as mixtures thereof, such as in particular from ethyl hexylsalicylate, homosalate, butyl methoxydibenzoylmethane and octocrylene.
  • Particularly suitable cosmetic oils to be incorporated into the oil phase of the topical sunscreen emulsions of the invention encompass Acetyl Tributyl Citrate, Bruxus (Jojoba Oil) Chinensis, Butylene Glycol Cocoate, Butylene Glycol Dicaprylate/Dicaprate,C12-13 AlkyI Ethylhexanoate,C12-13 AlkyI Lactate,C12-15 AlkyI Benzoate (and) Dipropylene Glycol Dibenzoate (and) PPG-15 Stearyl Ether Benzoate, C12-C15 alkyl benzoate [CAS 6841 1-27-8], C16-17 AlkyI Benzoate, Caprylic/Capric Triglyceride, Caprylyl Pyrrolidone, Cetearyl Isononanoate, Cetearyl Octanoate, Coco Caprylate/Caprate, Coco-Caprylate, Cocoglyceride, Cyclomethicone, Decyl Oleate, Dibut
  • Sesamum Indicum (Sesame) Seed Oil Squalane, Tributyl Citrate, Tri-C12-13 Alkyl Citrate, Trideceth-7, Tridecyl Salicylate, Tridecyl Trimellitate, Triethyl Citrate, Triethylhexanoin, Triisodecyl Trimellitate as well as mixtures thereof.
  • the amount of the water phase present in the topical sunscreen emulsions according to the invention is advantageously at least 30 wt.-%.
  • the amount of the water phase in all embodiments of the present invention is selected in the range of 40 to 90 wt.-%, more preferably in the range of 50 to 80 wt.-% and most preferably in the range of 55 to 75 wt.-% based on the total weight of the topical sunscreen emulsion.
  • the topical sunscreen emulsions according to the present invention in addition comprise an additional amount of ethanol.
  • the amount of ethanol is selected in the range of 1 to 15 wt.-%, more preferably in the range of 3 to 12 wt.-% and most preferably in the range of 5 to 10 wt.-% based on the total weight of the topical sunscreen emulsion.
  • the topical sunscreen emulsions according to the invention can be provided, for example, in the form of a serum, a milk, a lotion, a hydrodispersion, a foundation, a cream, a creamgel, which are prepared according to the usual methods.
  • the topical sunscreen emulsions according to the invention are advantageously in the form of an oil-in-water (O/W) emulsion comprising an oily phase dispersed in an aqueous phase in the presence of a phosphate ester emulsifier (i.e. an O/W emulsifier).
  • O/W emulsifier oil-in-water
  • the preparation of such O/W emulsions is well known to a person skilled in the art.
  • the invention relates to topical sunscreen emulsions with all the definitions and preferences given herein which are in the form of an O/W emulsion comprising an oily phase dispersed in an aqueous phase.
  • the O/W emulsion comprise potassium cetyl phosphate alone or potassium cetyl phosphate in combination with at least one further O/W emulsifier.
  • emulsifier potassium cetyl phosphate alone or photassium cetyl phosphate in combination with Polyglyceryl-3 Methylglucose Distearate or PEG-100 Stearate & Glyceryl Stearate is used.
  • potassium cetyl phosphate is used in combination with potassium cetyl phosphate is used in combination with
  • the topical compositions according to the invention furthermore advantageously contain at least one co-surfactant such as e.g. selected from the group of mono- and diglycerides and/ or fatty alcohols.
  • the co-surfactant is generally used in an amount selected in the range of 0.1 to 10 wt.-%, such as in particular in the range of 0.5 to 5 wt.-%, such as most in particular in the range of 1 to 3 wt.-%, based on the total weight of the composition.
  • Particular suitable co-surfactants are selected from the list of alkyl alcohols such as cetyl alcohol (Lorol C16, Lanette 16) cetearyl alcohol (Lanette O), stearyl alcohol (Lanette 18), behenyl alcohol (Lanette 22), glyceryl stearate, glyceryl myristate (Estol 3650), hydrogenated coco-glycerides (Lipocire Na10), acrylates/C 10-30 alkyl acrylate crosspolymer (Pemulen TR-2) as well as mixtures thereof.
  • alkyl alcohols such as cetyl alcohol (Lorol C16, Lanette 16) cetearyl alcohol (Lanette O), stearyl alcohol (Lanette 18), behenyl alcohol (Lanette 22), glyceryl stearate, glyceryl myristate (Estol 3650), hydrogenated coco-glycerides (Lipocire Na10), acrylates/C 10-30 alkyl acrylate
  • the topical sunscreen emulsions according to the invention in general have a pH in the range of 3 to 10, preferably a pH in the range of 4 to 8 and most preferably a pH in the range of 4 to 7.5.
  • the pH can easily be adjusted as desired with suitable acids such as e.g. citric acid or bases such as sodium hydroxide (e.g. as aqueous solution), Triethanolamine (TEA Care), Tromethamine (Trizma Base) and Aminomethyl Propanol (AMP-Ultra PC 2000) according to standard methods in the art.
  • the amount of the topical sunscreen emulsion to be applied to the skin is not critical and can easily be adjusted by a person skilled in the art.
  • the amount is selected in the range of 0.1 to 3 mg/ cm2 skin, such as preferably in the range of 0.1 to 2 mg/ cm2 skin and most preferably in the range of 0.5 to 2 mg / cm2 skin.
  • Example 1 Water resistance
  • the water resistance for each composition was determined as mean value from the 4 plates.
  • Viscarin PC 209 Chondrus Crispus 0.25 0.25 0.25
  • Euxyl PE 9010 Ethylhexylglycerin 1 .00 1 .00 1 .00 in vitro SPF initial 40 57 44 in vitro SPF after immersion
  • Viscosity 612 653 952 Table 2: O/W emulsion with 1.1 wt.-% Tego Care 450 & 0.5 wt.-% Amphisol ® K
  • Viscarin PC 209 Chondrus Crispus 0.20 0.20 0.20
  • Euxyl PE 9010 Ethylhexylglycerin 1 .00 1 .00 1 .00 in vitro SPF initial 49.2 49.4 49.9 in vitro SPF after immersion
  • Viscosity 512 1535 734 Table 4: O/W emulsion with 2.0wt.-% Tego Care 450 & 0.5 wt.-% Amphisol ® K
  • Euxyl PE 9010 Phenoxyethanol,Ethylhexylglycerin 1 .00 1 .00 in vitro SPF initial 41.4 46 in vitro SPF after immersion

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Emergency Medicine (AREA)
  • Dermatology (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Cosmetics (AREA)
PCT/EP2016/058931 2015-04-29 2016-04-21 Topical sunscreen emulsions WO2016173927A1 (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
JP2017555390A JP6798664B2 (ja) 2015-04-29 2016-04-21 局所日焼け止めエマルジョン
US15/568,557 US10709649B2 (en) 2015-04-29 2016-04-21 Topical sunscreen emulsions
ES16720758T ES2746287T3 (es) 2015-04-29 2016-04-21 Emulsiones tópicas de protección solar
EP16720758.8A EP3288525B1 (en) 2015-04-29 2016-04-21 Topical sunscreen emulsions
BR112017023041-0A BR112017023041B1 (pt) 2015-04-29 2016-04-21 emulsões tópicas de filtro solar, uso de fitantriol para aumentar a resistência à água de uma emulsão tópica de filtro solar e método para aumentar a resistência à água de pelo menos uma substância de filtro uv em uma emulsão tópica de filtro solar
KR1020177032576A KR20170141709A (ko) 2015-04-29 2016-04-21 국소 자외선 차단 유화액
CN201680024320.8A CN107530256B (zh) 2015-04-29 2016-04-21 局部用防晒乳剂

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP15165781 2015-04-29
EP15165781.4 2015-04-29

Publications (1)

Publication Number Publication Date
WO2016173927A1 true WO2016173927A1 (en) 2016-11-03

Family

ID=53040386

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2016/058931 WO2016173927A1 (en) 2015-04-29 2016-04-21 Topical sunscreen emulsions

Country Status (8)

Country Link
US (1) US10709649B2 (pt)
EP (1) EP3288525B1 (pt)
JP (1) JP6798664B2 (pt)
KR (1) KR20170141709A (pt)
CN (1) CN107530256B (pt)
BR (1) BR112017023041B1 (pt)
ES (1) ES2746287T3 (pt)
WO (1) WO2016173927A1 (pt)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2018155974A1 (ko) * 2017-02-27 2018-08-30 (주)아모레퍼시픽 블루라이트 필터링 및 자외선 차단 화장료 조성물
KR101899024B1 (ko) 2016-12-16 2018-11-05 주식회사 코리아나화장품 녹는 질감의 자외선 차단용 화장료 조성물
JP2018173327A (ja) * 2017-03-31 2018-11-08 株式会社コーセー 塗膜の耐水性評価方法
WO2019033584A1 (zh) * 2017-08-15 2019-02-21 广州无添加主义化妆品有限公司 一种防晒护肤品及其制备方法
WO2019192696A1 (en) * 2018-04-05 2019-10-10 Beiersdorf Ag Cosmetic composition for preconditioning the skin
WO2024124309A1 (en) * 2022-12-12 2024-06-20 L'oreal Cosmetic sunscreen composition and its use

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP7238225B2 (ja) * 2018-03-20 2023-03-14 ディーエスエム アイピー アセッツ ビー.ブイ. 局所用組成物
KR102130989B1 (ko) * 2019-12-17 2020-07-08 한국콜마주식회사 마크로 유화 입자를 포함하는 자외선 차단용 화장료 조성물
LU101670B1 (en) * 2020-03-09 2021-09-10 Soc De Recherche Cosmetique Sarl Sun protection topical composition
KR102358300B1 (ko) * 2021-10-28 2022-02-08 한국콜마주식회사 에어로졸 타입의 자외선 차단용 화장료 조성물
KR20230153946A (ko) * 2022-04-29 2023-11-07 주식회사 엘지생활건강 백탁 현상이 없는 자외선 차단용 화장료 조성물

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0711540A1 (fr) * 1994-11-10 1996-05-15 L'oreal Composition cosmétique ou dermatologique sous forme d'une dispersion d'une phase huileuse dans une phase aqueuse stabilisée à l'aide de particules de gel cubique et son procédé d'obtention
EP0884046A1 (en) * 1997-05-30 1998-12-16 Sara Lee/DE N.V. Cosmetic composition with photoprotective properties
EP1522303A1 (de) * 2003-10-10 2005-04-13 Cognis Deutschland GmbH & Co. KG Sonnenschutzmittel
WO2005048960A1 (en) * 2003-11-05 2005-06-02 Dsm Ip Assets B.V. Light protecting composition with reduced total amount of uv filter containing a polysiloxane-based uv filter
FR2899462A1 (fr) * 2006-04-06 2007-10-12 Oreal Emulsion huile dans eau a base de globules huileux pourvus d'un enrobage cristal liquide lamellaire contenant un filtre uv lipophile et le phytantriol sous forme de gel cubique ; utilisations
WO2009138485A1 (en) * 2008-05-16 2009-11-19 Dsm Ip Assets B.V. Sunscreens
DE102010063825A1 (de) 2010-12-22 2012-06-28 Beiersdorf Ag Kosmetische oder dermatologische wasserfeste Lichtschutzzubereitungen umfassend eine Kombination aus Polyacrylat- und Polyacrylamidverdicker

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5776443A (en) * 1996-03-18 1998-07-07 Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. Hair care compositions
DE19903459A1 (de) * 1999-01-28 2000-08-03 Basf Ag Verfahren zur Herstellung von hochreinem Phytantriol
AU774383B2 (en) * 1999-07-12 2004-06-24 Ciba Specialty Chemicals Holding Inc. Use of mixtures of micropigments for preventing tanning and for lightening skin and hair
EP1108417B1 (en) * 1999-12-16 2006-07-05 DSM IP Assets B.V. Hair colorant composition
FR2809954B1 (fr) * 2000-06-08 2004-03-12 Oreal Utilisation du phytantriol comme agent anti-pollution, notamment dans une composition cosmetique
DE10041220A1 (de) * 2000-08-22 2002-03-07 Basf Ag Hautkosmetische Formulierungen
DE10308565A1 (de) * 2003-02-25 2004-09-09 Symrise Gmbh & Co. Kg Universell einsetzbarer Emulgator vom Typ O/W basierend auf einem voll neutralisierten Phosphorsäureester und Palmglyceriden zur Herstellung von Cremes, Milchen und sehr niederviskosen, sprühfähigen Lotionen
EP1600210A1 (de) * 2004-05-25 2005-11-30 Cognis IP Management GmbH Beladene Mikrosphären
KR101390075B1 (ko) * 2009-07-07 2014-04-29 바스프 에스이 벤질리덴 말로네이트를 포함하는 uv 필터 조합물
WO2013103701A2 (en) * 2012-01-04 2013-07-11 Momentive Performance Materials Inc. Personal care compositions containing end-functionalized ionic silicone
WO2015123115A1 (en) * 2014-02-11 2015-08-20 Elc Management Llc Method, compositions, and kit for modulating the appearance of volume on keratin surfaces

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0711540A1 (fr) * 1994-11-10 1996-05-15 L'oreal Composition cosmétique ou dermatologique sous forme d'une dispersion d'une phase huileuse dans une phase aqueuse stabilisée à l'aide de particules de gel cubique et son procédé d'obtention
EP0884046A1 (en) * 1997-05-30 1998-12-16 Sara Lee/DE N.V. Cosmetic composition with photoprotective properties
EP1522303A1 (de) * 2003-10-10 2005-04-13 Cognis Deutschland GmbH & Co. KG Sonnenschutzmittel
WO2005048960A1 (en) * 2003-11-05 2005-06-02 Dsm Ip Assets B.V. Light protecting composition with reduced total amount of uv filter containing a polysiloxane-based uv filter
FR2899462A1 (fr) * 2006-04-06 2007-10-12 Oreal Emulsion huile dans eau a base de globules huileux pourvus d'un enrobage cristal liquide lamellaire contenant un filtre uv lipophile et le phytantriol sous forme de gel cubique ; utilisations
WO2009138485A1 (en) * 2008-05-16 2009-11-19 Dsm Ip Assets B.V. Sunscreens
DE102010063825A1 (de) 2010-12-22 2012-06-28 Beiersdorf Ag Kosmetische oder dermatologische wasserfeste Lichtschutzzubereitungen umfassend eine Kombination aus Polyacrylat- und Polyacrylamidverdicker

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
"SPF Boosters & Photostability of Ultraviolet Filters", HAPPI, October 2007 (2007-10-01), pages 77 - 83
DATABASE GNPD [online] MINTEL; 31 May 2010 (2010-05-31), "Retinol Complex", XP002744096, Database accession no. 1381258 *
NADIM A. SHAATH: "The Encyclopedia of Ultraviolet Filters"

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101899024B1 (ko) 2016-12-16 2018-11-05 주식회사 코리아나화장품 녹는 질감의 자외선 차단용 화장료 조성물
WO2018155974A1 (ko) * 2017-02-27 2018-08-30 (주)아모레퍼시픽 블루라이트 필터링 및 자외선 차단 화장료 조성물
KR20180098773A (ko) * 2017-02-27 2018-09-05 (주)아모레퍼시픽 유해 광선 차단 화장료 조성물
CN110494115A (zh) * 2017-02-27 2019-11-22 株式会社爱茉莉太平洋 用于过滤蓝光与阻隔紫外光的化妆品组合物
TWI771377B (zh) * 2017-02-27 2022-07-21 韓商愛茉莉太平洋股份有限公司 用於藍光過濾與紫外光阻隔的化妝品組合物
KR102672901B1 (ko) 2017-02-27 2024-06-10 (주)아모레퍼시픽 유해 광선 차단 화장료 조성물
JP2018173327A (ja) * 2017-03-31 2018-11-08 株式会社コーセー 塗膜の耐水性評価方法
WO2019033584A1 (zh) * 2017-08-15 2019-02-21 广州无添加主义化妆品有限公司 一种防晒护肤品及其制备方法
WO2019192696A1 (en) * 2018-04-05 2019-10-10 Beiersdorf Ag Cosmetic composition for preconditioning the skin
WO2024124309A1 (en) * 2022-12-12 2024-06-20 L'oreal Cosmetic sunscreen composition and its use

Also Published As

Publication number Publication date
KR20170141709A (ko) 2017-12-26
JP6798664B2 (ja) 2020-12-09
BR112017023041A2 (pt) 2018-07-03
EP3288525B1 (en) 2019-07-17
ES2746287T3 (es) 2020-03-05
CN107530256A (zh) 2018-01-02
JP2018514529A (ja) 2018-06-07
US10709649B2 (en) 2020-07-14
EP3288525A1 (en) 2018-03-07
BR112017023041B1 (pt) 2021-06-08
CN107530256B (zh) 2021-02-02
US20180110706A1 (en) 2018-04-26

Similar Documents

Publication Publication Date Title
US10709649B2 (en) Topical sunscreen emulsions
US11419804B2 (en) Sunscreen formulations optimized for the formation of vitamin D
KR101771754B1 (ko) 국소용 조성물
EP2945604B1 (en) Cosmetic or dermatological composition comprising a merocyanine and an oily phase comprising at least one specific amide compound
EP2956114B1 (en) Cosmetic or dermatological composition comprising a merocyanine, an oily phase and a c1-c4 monoalkanol
EP3709958A1 (en) Cosmetic or dermatological composition comprising a merocyanine and an acrylic polymer
EP2945601B1 (en) Cosmetic or dermatological composition comprising a merocyanine and a lipophilic benzotriazole uv-screening agent and/or a bis-resorcinyl triazine compound
EP2945605B1 (en) Cosmetic or dermatological composition comprising a merocyanine, an organic uvb-screening agent and an additional organic uva-screening agent
WO2014111568A1 (en) Cosmetic or dermatological water-in-oil emulsion comprising a merocyanine and at least one emulsifying polymer of the polyoxyalkylenated glycol fatty acid ester type
EP2945603B1 (en) Cosmetic or dermatological composition comprising a merocyanine and a uva-screening agent of the amino-substituted 2-hydroxybenzophenone type and/or a hydrophilic organic uva-screening agent
JP7424746B2 (ja) メロシアニンと、少なくとも1種のポリアルキレングリコールを含む油相とを含む化粧料組成物または皮膚科用組成物
JP7424747B2 (ja) メロシアニンと、少なくとも1種のイソソルビドエーテルを含む油相とを含む化粧料組成物または皮膚科用組成物
CN105705131A (zh) 包含部花青和不可溶的有机uv-遮蔽剂和/或不可溶的无机uv-遮蔽剂的化妆品或者皮肤病学组合物
EP3556748A1 (en) Hydroxyphenyl-triazine uv absorbers
WO2019096960A1 (en) Compositions comprising at least one acrylic polymer and at least one insoluble organic screening agent
EP3078397A1 (en) Topical sunscreen compositions

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 16720758

Country of ref document: EP

Kind code of ref document: A1

ENP Entry into the national phase

Ref document number: 2017555390

Country of ref document: JP

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: 15568557

Country of ref document: US

NENP Non-entry into the national phase

Ref country code: DE

ENP Entry into the national phase

Ref document number: 20177032576

Country of ref document: KR

Kind code of ref document: A

REG Reference to national code

Ref country code: BR

Ref legal event code: B01A

Ref document number: 112017023041

Country of ref document: BR

ENP Entry into the national phase

Ref document number: 112017023041

Country of ref document: BR

Kind code of ref document: A2

Effective date: 20171025